chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	104442503	104442504	G	A	14	GENIC	homozygous	61490089
1	104443196	104443197	T	A	33	GENIC	homozygous	61490090
1	104443201	104443202	G	A	32	GENIC	homozygous	61490091
1	104444004	104444005	A	C	20	GENIC	homozygous	61490092
1	104444174	104444175	A	AGTGTGTGTGTGTGTGT	7	GENIC	possibly homozygous	62147949
1	104445688	104445689	G	GA	5	GENIC	homozygous	61490094
1	104445879	104445880	A	C	13	GENIC	homozygous	61490095
1	104446521	104446522	A	AACACACACAC	1	GENIC	homozygous	62553631
1	104446762	104446763	T	TACACACACACACAC	14	GENIC	homozygous	62311849
1	104447099	104447100	A	C	13	GENIC	homozygous	61490098
1	104447449	104447450	A	G	12	GENIC	homozygous	61490099
1	104447689	104447709	CACACACACACACACACACA	--------------------	13	GENIC	homozygous	61490100
1	104448784	104448785	C	T	31	GENIC	homozygous	61490101
1	104448794	104448795	G	A	29	GENIC	homozygous	61490102
1	104448836	104448837	G	A	30	GENIC	homozygous	61490103
1	104448899	104448900	G	A	25	GENIC	homozygous	61490104
1	104449762	104449764	CA	--	6	GENIC	heterozygous	62147955
1	104450129	104450130	A	AT	18	GENIC	possibly homozygous	61490105
1	104450351	104450352	A	C	23	GENIC	homozygous	61490106
1	104450391	104450392	T	C	26	GENIC	homozygous	61490107
1	104450737	104450738	A	C	22	GENIC	homozygous	61490108